全文获取类型
收费全文 | 7636篇 |
免费 | 799篇 |
国内免费 | 3篇 |
出版年
2023年 | 68篇 |
2022年 | 47篇 |
2021年 | 260篇 |
2020年 | 169篇 |
2019年 | 232篇 |
2018年 | 195篇 |
2017年 | 202篇 |
2016年 | 314篇 |
2015年 | 545篇 |
2014年 | 593篇 |
2013年 | 601篇 |
2012年 | 785篇 |
2011年 | 728篇 |
2010年 | 401篇 |
2009年 | 358篇 |
2008年 | 455篇 |
2007年 | 416篇 |
2006年 | 344篇 |
2005年 | 304篇 |
2004年 | 278篇 |
2003年 | 208篇 |
2002年 | 172篇 |
2001年 | 71篇 |
2000年 | 61篇 |
1999年 | 54篇 |
1998年 | 33篇 |
1997年 | 26篇 |
1996年 | 18篇 |
1995年 | 17篇 |
1994年 | 15篇 |
1992年 | 20篇 |
1991年 | 24篇 |
1990年 | 26篇 |
1989年 | 30篇 |
1988年 | 20篇 |
1987年 | 19篇 |
1986年 | 12篇 |
1985年 | 24篇 |
1984年 | 18篇 |
1983年 | 15篇 |
1982年 | 16篇 |
1981年 | 15篇 |
1980年 | 16篇 |
1979年 | 18篇 |
1977年 | 14篇 |
1976年 | 13篇 |
1975年 | 10篇 |
1974年 | 16篇 |
1972年 | 9篇 |
1970年 | 12篇 |
排序方式: 共有8438条查询结果,搜索用时 109 毫秒
1.
Jessica Hanser 《Curtis's Botanical Magazine》2017,34(4):314-322
This essay reveals a financial dimension to Captain John Blake and his son John Bradby Blake's involvement with China, namely, their participation in financing the Canton trade through predatory loans to Chinese Hong merchants. Widespread predatory lending in Canton led to a financial crisis during the late 1770s, which ruined several British and Chinese merchants. In an effort to recover the money they claimed was owed to them, many British traders, including John Blake, formed a lobby group in London and authorized Britain's first Ambassador to China to negotiate with the Emperor in Beijing on their behalf. 相似文献
2.
3.
4.
5.
Summary Two previously identified forms of macrophage were investigated in primary cultures of cerebral cortical cells. Dynamic features were revealed through time-lapse video recording and aspects of macrophage function were assessed. The two cell forms were shown to be different pre-mitotic stages of a single cell type. The cell cycle for these cells involved an initial large, flat, quiescent cell which retracted to yield a slightly rounded form with numerous processes. This latter form lost processes and developed profuse filopodia as it became very rounded just prior to division; both resulting daughter cells then regained the initial large flat appearance. These cells possessed several properties of macrophages, including phagocytosis, nucleoside diphosphatase enzyme, and CR3 receptors. These properties were transient, expressed just before and after mitosis, but subsequently down-regulated in the flat daughter cells. Because of this feature, it was difficult to determine the exact size of this cell population; however, the observed rate of proliferation suggests it may be substantial. It is suggested that these cells correspond to non-microglial macrophages of brain tissue and, because of their significant down-regulation, they may be difficult to detect. This may be important in studies of brain accessory immune cells in tissue culture. 相似文献
6.
7.
8.
9.
Jonathan T. Sims Sourik S. Ganguly Holly Bennett J. Woodrow Friend Jessica Tepe Rina Plattner 《PloS one》2013,8(1)
Despite advances in cancer detection and prevention, a diagnosis of metastatic disease remains a death sentence due to the fact that many cancers are either resistant to chemotherapy (conventional or targeted) or develop resistance during treatment, and residual chemoresistant cells are highly metastatic. Metastatic cancer cells resist the effects of chemotherapeutic agents by upregulating drug transporters, which efflux the drugs, and by activating proliferation and survival signaling pathways. Previously, we found that c-Abl and Arg non-receptor tyrosine kinases are activated in breast cancer, melanoma, and glioblastoma cells, and promote cancer progression. In this report, we demonstrate that the c-Abl/Arg inhibitor, imatinib (imatinib mesylate, STI571, Gleevec), reverses intrinsic and acquired resistance to the anthracycline, doxorubicin, by inducing G2/M arrest and promoting apoptosis in cancer cells expressing highly active c-Abl and Arg. Significantly, imatinib prevents intrinsic resistance by promoting doxorubicin-mediated NF-κB/p65 nuclear localization and repression of NF-κB targets in a STAT3-dependent manner, and by preventing activation of a novel STAT3/HSP27/p38/Akt survival pathway. In contrast, imatinib prevents acquired resistance by inhibiting upregulation of the ABC drug transporter, ABCB1, directly inhibiting ABCB1 function, and abrogating survival signaling. Thus, imatinib inhibits multiple novel chemoresistance pathways, which indicates that it may be effective in reversing intrinsic and acquired resistance in cancers containing highly active c-Abl and Arg, a critical step in effectively treating metastatic disease. Furthermore, since imatinib converts a master survival regulator, NF-κB, from a pro-survival into a pro-apoptotic factor, our data suggest that NF-κB inhibitors may be ineffective in sensitizing tumors containing activated c-Abl/Arg to anthracyclines, and instead might antagonize anthracycline-induced apoptosis. 相似文献
10.